chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207155330207155331CCTGG13GENIChomozygous62202680
2207155910207155911GC33GENICpossibly homozygous62202682
2207156238207156239TC24GENIChomozygous59354874
2207158266207158267AG19GENIChomozygous62202684
2207158966207158967GC29GENIChomozygous59354877
2207159585207159586CT16GENIChomozygous59354879
2207159780207159781GA37GENICpossibly homozygous59930945
2207160329207160330T-15GENIChomozygous60825865
2207163032207163046TCTCTCTCTCTCTC--------------4GENICheterozygous62202688
2207163387207163388TC40GENIChomozygous62202690
2207164055207164065AGAGAGAGAG----------12GENIChomozygous62202692
2207165379207165380CCAAAA7GENICheterozygous59354905
2207165379207165380CCA7GENICheterozygous59354907
2207165379207165380CCAAAAA7GENICheterozygous60561209
2207165379207165380CCAA7GENICheterozygous61601509
2207165540207165541GT17GENIChomozygous62202694
2207168320207168321CT24GENIChomozygous62202696
2207168943207168945AA--4GENIChomozygous62202698
2207170466207170467GA32GENICpossibly homozygous62202700
2207171693207171694TC20GENICpossibly homozygous62202702
2207171710207171711TC17GENICpossibly homozygous62202704
2207171725207171726AG21GENICpossibly homozygous62202706
2207171795207171796TG28GENICheterozygous59354918
2207173445207173446T-11GENIChomozygous62202708
2207173790207173791A-9GENICpossibly homozygous60514500